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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 639372Erstellt: 26. Oktober 2026

1-(2-Chloroethoxy)-4-nitrobenzene → 4-(2-Chloroethoxy)aniline

https://huagongshe.com/reaction/639372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2-Chloroethoxy)-4-nitrobenzeneHCID 2764587—
KatalysatorAdams' catalystHCID 345198—
LösungsmittelEthanolHCID 702—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-Chloroethoxy)anilineHCID 119699—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

36 g (0.178 Mol) of 1-(2-Chloro-ethoxy)-4-nitro-benzene is dissolved in 360 mL of ethanol and subjected to catalytic hydration at rt using PtO2 (1.5 g) as catalyst. The resulting suspension is diluted with CH2Cl2, filtered, and concentrated to approx. 150 mL. After cooling to 0° C. the crystals are filtered off, washed and dried at 60° C. under vacuum to obtain 4-(2-chloro-ethoxy)-phenylamine. Title compound: m.p.: 87-91° C.; ES-MS: 172 [M+H]+; single peak at tR=2.73 min (System 1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07691855B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-49fe89710516443cb85d5cc9e60bff6f
Quellennotizuspto-grants-2010_04